乙苯
催化作用
双金属片
氧化还原
煅烧
苯乙酮
化学
产量(工程)
化学工程
氧化物
材料科学
无机化学
有机化学
工程类
冶金
作者
Jiangyong Liu,Wanjing Wang,Panming Jian,Lixia Wang,Xiaodong Yan
标识
DOI:10.1016/j.jcis.2022.01.108
摘要
Herein, we developed a series of CeVO4 samples with hierarchical hollow microsphere-like structure obtained at different calcination temperatures for the selective oxidation of ethylbenzene (EB) to acetophenone (AcPO) in the presence of TBHP. The optimized catalyst (CVO-500) exhibits a very high yield value of 95.0% (initial reaction rate of 49.4 mmol gcat-1 h-1) under the optimal reaction conditions. Importantly, the representative CVO-500 catalyst presents high stability, with the reaction performance well maintained after five consecutive uses. It has been indicated that the redox V5+/V3+ sites serve as the main active centers, while the electronic interaction and redox transformation between Ce and V facilitates the hopping of V5+/V3+ and the generation of oxygen vacancies. The bimetallic synergy between V and Ce thus endows the CVO-500 catalyst an excellent performance in the EB oxidation reaction. This work paves the way for the exploit of high-performance and cost-effective catalyst for the EB oxidation and beyond.
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